Qualified person responsible for information and publicity (qp rip)
Local contact person for pharmacovigilance (lppv)
Regulatory intelligence
The Pharmaceutical Affairs Associate Director acts as the Qualified Person Responsible for Information and Publicity (QP RIP) and is responsible for medical information and publicity in Belgium and Luxembourg
Job Summary
The Pharmaceutical Affairs Associate Director acts as the Qualified Person Responsible for Information and Publicity (QP RIP) and is responsible for medical information and publicity in Belgium and Luxembourg.
As Pharmaceutical affairs Associate Director, he (she) also steers locally the quality, regulatory and compliance activities within the affiliate and in collaboration with EU departments in accordance with Belgian, Dutch and Luxembourg laws and regulations.
The role involves fulfilling the duties of the employer designated Prevention advisor in line with Belgium regulation and overseeing the legally required, repeated risk analysis.
Matching Summary
The Pharmaceutical Affairs Associate Director acts as the Qualified Person Responsible for Information and Publicity (QP RIP) and is responsible for medical information and publicity in Belgium and Luxembourg.
Skills & Requirements
Must-have
Qualified Person Responsible for Information and Publicity (QP RIP)
Local contact Person for Pharmacovigilance (LPPV)
Regulatory intelligence
Medical information management
Promotional and medical material review
Drug safety management
Compliance management
Nice-to-have
Collaborative Spirit
Bold Ingenuity
Driving Excellence
Patients First
Agile, strategic thinking
Out-of-the-box thinking
Key Requirements
Minimum of 10 years of pharmaceutical industry/biotech in regulatory affairs in Belgium
Certified Prevention Adviser Level III
Fluent in English, French or Dutch
Oncology market experience strongly preferred
PharmD or PhD, or Bachelor of Science, Master’s in Science or Business